Laffan J, Firshein W
J Bacteriol. 1987 Sep;169(9):4135-40. doi: 10.1128/jb.169.9.4135-4140.1987.
Binding of membrane proteins extracted from Bacillus subtilis to an 11.6-kilobase region containing the origin of replication was examined by Western blotting (protein blotting) procedures. Two adjacent origin probes in the double-stranded form (spanning a length of 4 kilobases) were found to bind very strongly to a 63-kilodalton (kDa) protein in that they resisted dissociation after a high-concentration salt wash. This region encompasses both a site implicated in initiation in vivo and a gene coding for a DNA gyrase subunit (gyrA). In contrast, flanking origin and nonorigin double-stranded probes were dissociated after washing with a high salt concentration. Another protein of 67 kDa bound less intensely to the putative initiation site but not to the gyrA region. All of the origin and nonorigin probes in the double- or single-stranded form were found to bind nonspecifically to a subset of 10 to 12 proteins of 50 to 60 separated by gel electrophoresis after a low-concentration salt wash. They ranged in size from 14 to over 100 kDa (including 63 kDa). However, in contrast to the double-stranded forms, most of the single-stranded probes resisted dissociation from the protein subset after a high-concentration salt wash.
通过蛋白质印迹法检测了从枯草芽孢杆菌中提取的膜蛋白与包含复制起点的11.6千碱基区域的结合情况。发现两个相邻的双链形式的起点探针(跨度为4千碱基)与一种63千道尔顿(kDa)的蛋白质紧密结合,因为在高浓度盐洗后它们仍能抵抗解离。该区域既包含一个与体内起始相关的位点,也包含一个编码DNA促旋酶亚基(gyrA)的基因。相比之下,侧翼起点和非起点双链探针在高盐浓度洗涤后会解离。另一种67 kDa的蛋白质与假定的起始位点结合较弱,但不与gyrA区域结合。在低浓度盐洗后,发现双链或单链形式的所有起点和非起点探针都能非特异性地与凝胶电泳分离的10至12种50至60 kDa的蛋白质亚群结合。它们的大小范围从14 kDa到超过100 kDa(包括63 kDa)。然而,与双链形式不同的是,大多数单链探针在高浓度盐洗后仍能抵抗从蛋白质亚群中解离。